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KCNQ4 Mouse anti-Human, Mouse, Rat, Clone: S43-6, Invitrogen™

Mouse Monoclonal Antibody

Manufacturer:  Invitrogen MA527653

Catalog No. PIMA527653

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The protein encoded by this gene forms a potassium channel that is thought to play a critical role in the regulation of neuronal excitability, particularly in sensory cells of the cochlea. The current generated by this channel is inhibited by M1 muscarinic acetylcholine receptors and activated by retigabine, a novel anti-convulsant drug. The encoded protein can form a homomultimeric potassium channel or possibly a heteromultimeric channel in association with the protein encoded by the KCNQ3 gene. Defects in this gene are a cause of nonsyndromic sensorineural deafness type 2, an autosomal domit form of progressive hearing loss. Two transcript variants encoding different isoforms have been found for this gene.


1 mg/ml
PBS with 50% glycerol and 0.09% sodium azide; pH 7.4
P56696, Q9JK96, Q9JK97
DFNA 2, DFNA2, KCNQ 4, Kcnq4, KCNQ4_HUMAN, KQT like 4, KQT-like 4, KV7.4, Potassium channel KQT like 4, Potassium channel subunit alpha KvLQT4, Potassium voltage gated channel KQT like protein 4, Potassium voltage gated channel KQT like subfamily member 4, Potassium voltage gated channel subfamily KQT member 4, Potassium voltage-gated channel subfamily KQT member 4, Voltage gated potassium channel subunit Kv7.4, Voltage-gated potassium channel subunit Kv7.4
100 μg
298496, 60613, 9132
Immunocytochemistry, Immunofluorescence, Immunohistochemistry (Paraffin), Immunoprecipitation, Western Blot
Fusion protein amino acids 2-77 of human KCNQ4
Protein G
Human, Mouse, Rat
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